Facile Synthesis of Oxime Amino Ethers via Lewis Acid Catalyzed S N 2-Type Ring Opening of Activated Aziridines with Aryl Aldehyde Oximes

Aditya Bhattacharyya; Subhomoy Das; Navya Chauhan; Pronay K. Biswas; Manas K. Ghorai

doi:10.1055/s-0039-1691596

Facile Synthesis of Oxime Amino Ethers via Lewis Acid Catalyzed S _N 2-Type Ring Opening of Activated Aziridines with Aryl Aldehyde Oximes

Aditya Bhattacharyya, Subhomoy Das, Navya Chauhan, Pronay K. Biswas, Manas K. Ghorai

Indian Institute of Technology Kanpur

Research output: Contribution to journal › Article › peer-review

6 Scopus citations

Abstract

A simple strategy to access a wide range of substituted oxime amino ethers in good to high yields via Lewis acid catalyzed S _N 2-type ring opening of activated aziridines with aryl aldehyde oximes is reported.

Original language	English
Pages (from-to)	708-712
Number of pages	5
Journal	Synlett
Volume	31
Issue number	7
DOIs	https://doi.org/10.1055/s-0039-1691596
State	Published - 22 Apr 2020
Externally published	Yes

Bibliographical note

Publisher Copyright:
© 2020 Georg Thieme Verlag. All rights reserved.

Funding

M.K.G. is thankful to the Department of Science and Technology (DST), India for financial support. A.B. thanks the Council of Scientific and Industrial Research (CSIR), New Delhi, India for a research fellowship. S.D. and N.C. thank University Grants Commission (UGC), New Delhi, India for Senior Research Fellowships. DepartmentofScienceandTechnology(DST)()IndianInstituteofChemicalBiology()

Funders	Funder number
Department of Science and Technology, Ministry of Science and Technology, India
Council of Scientific and Industrial Research, India
University Grants Commission

Keywords

Lewis acid catalyst
S 2-type ring opening
aziridine
oxime
oxime ether
stereoselectivity

Access to Document

10.1055/s-0039-1691596

Cite this

@article{fdb0a229da7b46238263e37401a49f1f,

title = "Facile Synthesis of Oxime Amino Ethers via Lewis Acid Catalyzed S N 2-Type Ring Opening of Activated Aziridines with Aryl Aldehyde Oximes",

abstract = "A simple strategy to access a wide range of substituted oxime amino ethers in good to high yields via Lewis acid catalyzed S N 2-type ring opening of activated aziridines with aryl aldehyde oximes is reported.",

keywords = "Lewis acid catalyst, S 2-type ring opening, aziridine, oxime, oxime ether, stereoselectivity",

author = "Aditya Bhattacharyya and Subhomoy Das and Navya Chauhan and Biswas, {Pronay K.} and Ghorai, {Manas K.}",

year = "2020",

month = apr,

day = "22",

doi = "10.1055/s-0039-1691596",

language = "אנגלית",

volume = "31",

pages = "708--712",

journal = "Synlett",

issn = "0936-5214",

publisher = "Georg Thieme Verlag",

number = "7",

}

TY - JOUR

T1 - Facile Synthesis of Oxime Amino Ethers via Lewis Acid Catalyzed S N 2-Type Ring Opening of Activated Aziridines with Aryl Aldehyde Oximes

AU - Bhattacharyya, Aditya

AU - Das, Subhomoy

AU - Chauhan, Navya

AU - Biswas, Pronay K.

AU - Ghorai, Manas K.

PY - 2020/4/22

Y1 - 2020/4/22

N2 - A simple strategy to access a wide range of substituted oxime amino ethers in good to high yields via Lewis acid catalyzed S N 2-type ring opening of activated aziridines with aryl aldehyde oximes is reported.

AB - A simple strategy to access a wide range of substituted oxime amino ethers in good to high yields via Lewis acid catalyzed S N 2-type ring opening of activated aziridines with aryl aldehyde oximes is reported.

KW - Lewis acid catalyst

KW - S 2-type ring opening

KW - aziridine

KW - oxime

KW - oxime ether

KW - stereoselectivity

UR - http://www.scopus.com/inward/record.url?scp=85082692662&partnerID=8YFLogxK

U2 - 10.1055/s-0039-1691596

DO - 10.1055/s-0039-1691596

M3 - ???researchoutput.researchoutputtypes.contributiontojournal.article???

AN - SCOPUS:85082692662

SN - 0936-5214

VL - 31

SP - 708

EP - 712

JO - Synlett

JF - Synlett

IS - 7

ER -